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Topic:Contagious Equine Metritis

Contagious Equine Metritis (CEM) is a venereal disease in horses caused by the bacterium Taylorella equigenitalis. It primarily affects the reproductive tract of mares, leading to inflammation and potentially impacting fertility. Stallions can carry the bacterium asymptomatically, acting as vectors for transmission during breeding. Diagnosis of CEM involves bacterial culture, polymerase chain reaction (PCR) testing, and serological assays. Control measures include quarantine, testing, and treatment of infected animals. This page compiles peer-reviewed research studies and scholarly articles that investigate the epidemiology, pathogenesis, diagnostic methods, and management strategies for Contagious Equine Metritis in equine populations.
Identification of Taylorella equigenitalis responsible for contagious equine metritis in equine genital swabs by direct polymerase chain reaction.
Research in veterinary science    June 27, 2006   Volume 82, Issue 1 47-49 doi: 10.1016/j.rvsc.2006.05.001
Duquesne F, Pronost S, Laugier C, Petry S.A direct-PCR assay was developed for the rapid detection of Taylorella equigenitalis, a Gram-negative bacterium responsible for contagious equine metritis (CEM) in Equidae. The bacteria may be detected in equine genital swabs without need for a preliminary step of DNA extraction or bacterial isolation. Specificity was determined with 125 isolates of T. equigenitalis, 24 isolates of Taylorella asinigenitalis, five commensal bacteria of the genital tract and a facultative intracellular pathogen of foals found in large concentration in soil. Our PCR is specific and amplified a 413-bp 16S ribosoma...
Isolation and identification of Taylorella asinigenitalis from the genital tract of a stallion, first case of a natural infection.
Veterinary microbiology    May 7, 2006   Volume 116, Issue 4 294-300 doi: 10.1016/j.vetmic.2006.04.027
Båverud V, Nyström C, Johansson KE.Contagious equine metritis (CEM), caused by Taylorella equigenitalis, is a widely known highly contagious genital equine disease that is transmitted venereally. A new bacterium, Taylorella asinigenitalis resembling T. equigenitalis was recently isolated from three American donkey jacks, at routine testing for CEM. The purpose of this study was to identify and characterize a strain of Taylorella sp. from the genital tract of a stallion. Swab samples for culture of T. equigenitalis were taken from urethral fossa, urethra and penile sheath of a 3-year-old stallion of the Ardennes breed when it wa...
Quantitative assessment of the risks of reducing the routine swabbing requirements for the detection of Taylorella equigenitalis.
The Veterinary record    July 12, 2005   Volume 157, Issue 2 41-46 doi: 10.1136/vr.157.2.41
Wood JL, Kelly L, Cardwell JM, Park AW.The transmission of contagious equine metritis (CEM) on stud farms in Britain, Ireland and other European countries is prevented by following the recommendations in the Horserace Betting Levy Board's Code of Practice on CEM. A quantitative risk assessment was undertaken to estimate the likely impact of removing the recommendation, from the 2002 code, to culture endometrial or cervical swabs microaerophilically for the presence of Taylorella equigenitalis, the causative organism. The scientific literature was reviewed for evidence about the anatomical distribution of T. equigenitalis at differe...
Prevalence of Taylorella equigenitalis infection in stallions in Slovenia: bacteriology compared with PCR examination.
Equine veterinary journal    May 17, 2005   Volume 37, Issue 3 217-221 doi: 10.2746/0425164054530696
Zdovc I, Ocepek M, Gruntar I, Pate M, Klobucar I, Krt B.The prevalence of Taylorella equigenitalis infection in Slovenia is unknown and methods used to refine identification in these stallions are required. Objective: In diagnosis of T. equigenitalis, polymerase chain reaction (PCR) would have advantages over culture methods, especially in cases where small numbers of causal agent or intensive contamination of genital swabs are involved. Methods: Culture method and PCR were used to examine a total of 980 genital swabs from the urethra and fossa urethralis of 245 stallions for the presence of the contagious equine metritis organism. Results: Among 2...
A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses.
Irish veterinary journal    March 1, 2005   Volume 58, Issue 3 146-149 doi: 10.1186/2046-0481-58-3-146
Buckley TC, Millar BC, Egan CL, Gibson P, Cosgrove H, Stanbridge S, Matsuda M, Moore JE.: A two-step PCR assay was developed for the molecular detection of Taylorella equigenitalis, a Gram-negative genital bacterial pathogen in horses. Two specific oligonucleotide primers (TE16SrRNABCHf [25mer] and TE16SrRNABCHr [29mer]) were designed from multiple alignments of the 16S rRNA gene loci of several closely related taxa, including T. asinigenitalis. Subsequent enhanced surveillance of 250 Thoroughbred animals failed to detect the presence of this organism directly from clinical swabs taken from the genital tract of mares and stallions. Such a molecular approach offers a sensitive and...
Diagnosis and treatment of four stallions, carriers of the contagious metritis organism–case report.
Theriogenology    December 10, 2003   Volume 61, Issue 2-3 595-601 doi: 10.1016/s0093-691x(03)00228-0
Kristula MA, Smith BI.Contagious Equine Metritis (CEM), a venereal disease of horses caused by the bacterium Taylorella equigenitalis, was first diagnosed in 1977 and subsequently spread to many nations [Proc 24th AM Assoc Equine Pract (1979) 287]. The disease was confirmed in the United States in 1978 [Proc Am Assoc Equine Pract (1983) 295]. Specific regulatory procedures for this disease have been established in the United States and 37 other countries. From 1999 through 2001, four of 120 imported European stallions tested positive for CEM at a quarantine facility in Darlington, MD, USA. Two stallions were identi...
Recent advances in molecular epidemiology and detection of Taylorella equigenitalis associated with contagious equine metritis (CEM).
Veterinary microbiology    November 26, 2003   Volume 97, Issue 1-2 111-122 doi: 10.1016/j.vetmic.2003.08.001
Matsuda M, Moore JE.In the present review article, recent molecular advances relating to studies with Taylorella equigenitalis, as well as the recently described second species of the genus Taylorella, namely Taylorella asinigenitalis, have been described. Molecular genotyping of T. equigenitalis strains by pulsed-field gel electrophoresis (PFGE) after digestion with the suitable restriction enzyme(s) enabled the effective discrimination of strains, thus allowing the examination of the scientific mechanism(s) for its occurrence and transmission of contagious equine metritis (CEM). Alternatively, polymerase chain ...
Evaluation of the field application of PCR in the eradication of contagious equine metritis from Japan.
The Journal of veterinary medical science    December 25, 2002   Volume 64, Issue 11 999-1002 doi: 10.1292/jvms.64.999
Anzai T, Wada R, Okuda T, Aoki T.The effectiveness of the polymerase chain reaction (PCR) as a field application test for the eradication of contagious equine metritis (CEM) was evaluated. Seven-thousands five-hundred and thirty-four genital swabs were collected from 4,026 Thoroughbred broodmares and stallions in Japan to test "high risk" horses as well as for general surveillance testing from 1998 to 2001. Bacterial isolation as well as PCR testing of original specimens and cultured specimens was performed for detection of Taylorella equigenitalis from genital swabs. As a result, T. equigenitalis was detected in 12 mares and...
The role of international transport of equine semen on disease transmission.
Animal reproduction science    December 18, 2001   Volume 68, Issue 3-4 229-237 doi: 10.1016/s0378-4320(01)00159-2
Metcalf ES.Despite the numerous benefits of having the capability to transport semen internationally, there are serious potential ramifications if that semen is contaminated with a communicable disease. Bacteria: Many commensal bacteria colonize the exterior of the stallion penis and are not regarded as pathogenic. They may be cultured from an ejaculate. Alterations of the normal bacterial flora on the exterior genitalia may cause the growth of opportunistic bacteria such as Klebsiella pneumonia, Pseudomonas aeruginosa, Streptococcus zooepidemicus, which, if inseminated, may cause infertility in suscepti...
Demonstration of heterogeneous genotypes of Taylorella equigenitalis isolated from horses in six European countries by pulsed-field gel electrophoresis.
Veterinary research communications    October 5, 2001   Volume 25, Issue 7 565-575 doi: 10.1023/a:1017925216350
Kagawa S, Klein F, Corboz L, Moore JE, Murayama O, Matsuda M.Forty-six isolates of Taylorella equigenitalis were analysed by pulsed-field gel electrophoresis (PFGE) after separate digestion of the genomic DNA with ApaI and with NotI. The isolates had been obtained from horses in six European countries and were classified into 18 genotypes. In Belgium, 2 genotypes were detected in 2 isolates, in England 9 among 15, in Finland 2 in 2, in France 2 among 10, in Sweden 3 among 5, and in Switzerland 3 among 12. Two English isolates and 4 French isolates gave identical PFGE profiles to those of Kentucky 188 from the United States. A common genotype was found i...
Contagious equine metritis in Turkey: first isolation of Taylorella equigenitalis from mares.
The Veterinary record    August 16, 2001   Volume 149, Issue 4 120-122 doi: 10.1136/vr.149.4.120
Ozgur NY, Ikiz S, Carioglu B, Kilicarslan R, Yilmaz H, Akay O, Ilgaz A.No abstract available
Multiplex polymerase chain reaction for distinguishing Taylorella equigenitalis from Taylorella equigenitalis-like organisms. Arata AB, Cooke CL, Jang SS, Hirsh DC.It is difficult to distinguish isolates of Taylorella equigenitalis, the cause of contagious equine metritis, from a T. equigenitalis-like organism isolated from asymptomatic donkeys and horses. Although T. equigenitalis is responsible for a severe, contagious disease of the reproductive tract of equids, the T. equigenitalis-like organism, although contagious, does not appear to produce disease. Because of the economic consequences of correctly distinguishing isolates of these 2 microorganisms, a polymerase chain reaction (PCR)-based assay was developed that will distinguish isolates of T. equ...
Comparison of the value of pulsed-field gel electrophoresis, random amplified polymorphic DNA and amplified rDNA restriction analysis for subtyping Taylorella equigenitalis.
Veterinary research communications    July 4, 2001   Volume 25, Issue 4 261-269 doi: 10.1023/a:1010674524428
Kagawa S, Moore JE, Murayama O, Matsuda M.Eight strains of Taylorella equigenitalis were identified by a polymerase chain reaction using a primer pair specific to the 16S rDNA of T equigenitalis. These eight strains were chosen because they had previously been shown to represent eight distinct genotypes by pulsed-field gel electrophoresis analysis after separate digestion of the genomic DNA with ApaI or NotI. The eight strains could be classified into six or seven types by random amplified polymorphic DNA analysis using different kinds of primers. Amplified rDNA restriction analysis after separate digestion with five restriction enzym...
Molecular surveillance of the incidence of Taylorella equigenitalis and Pseudomonas aeruginosa from horses in Ireland by sequence-specific PCR.
Equine veterinary journal    May 16, 2001   Volume 33, Issue 3 319-322 doi: 10.2746/042516401776249750
Moore JE, Buckley TC, Millar BC, Gibson P, Cannon G, Egan C, Cosgrove H, Stanbridge S, Anzai T, Matsuda M, Murphy PG.No abstract available
An enzyme-linked immunosorbent assay for the convenient serodiagnosis of contagious equine metritis in mares. Katz J, Geer P.An enzyme-linked immunosorbent assay (ELISA) was developed for the serodiagnosis of contagious equine metritis (CEM), a sexually transmitted disease caused by Taylorella equigenitalis. Antigen preparation was simple, and antigens derived from both classical and atypical forms of T. equigenitalis enabled detection of antibody responses elicted in horses experimentally exposed to either form of the bacterium. Sera serially obtained from these horses from 0 to 63 days postexposure were tested by the traditional complement fixation test (CFT) for CEM and with the ELISA, using both antigens separat...
Development of a PCR test for rapid diagnosis of contagious equine metritis.
The Journal of veterinary medical science    January 29, 2000   Volume 61, Issue 12 1287-1292 doi: 10.1292/jvms.61.1287
Anzai T, Eguchi M, Sekizaki T, Kamada M, Yamamoto K, Okuda T.In order to establish a rapid diagnostic method for contagious equine metritis (CEM), we developed and evaluated a polymerase chain reaction (PCR) test. Species-specific PCR primer sets were derived from the DNA sequence of a cloned DNA fragment of Taylorella equigenitalis that did not hybridize with the genome of a taxomonically related species, Oligella urethralis. Single step PCR with primer set P1-N2 and two-step semi-nested PCR with primer sets P1-N2 and P2-N2 detected as low as 100 and 10 CFU of the bacteria, respectively. Single-step PCR detected T. equigenitalis from genital swabs of e...
Detection of a common genotype among strains of Taylorella equigenitalis isolated from thoroughbred horses in Japan between 1994 and 1996.
Journal of basic microbiology    May 21, 1999   Volume 39, Issue 2 127-130 doi: 10.1002/(sici)1521-4028(199905)39:23.0.co;2-q
Matsuda M, Miyazawa T, Anzai T.We examined whether or not the genotype J could be detected among 21 new strains of T. equigenitalis isolated between 1994 and 1996 in Japan since our previous report (MIYAZAWA et al. 1995). The respective pulsed-field gel electrophoretic profiles of the 21 Japanese strains, as well as those of an old EQ59 used as a reference strain after separate digestion with the two restriction enzymes, ApaI and NotI, were essentially identical but differed from those of T. equigenitalis NCTC11184T and KENTUCKY 188, respectively. Hence, the 21 strains and EQ59 appeared to have a common genotype J. Conseque...
Use of a PCR assay for Taylorella equigenitalis applied to samples from the United Kingdom.
The Veterinary record    October 15, 1998   Volume 143, Issue 8 225-227 doi: 10.1136/vr.143.8.225
Chanter N, Vigano F, Collin NC, Mumford JA.No abstract available
[Reproduction in horses: contagious equine endometritis (CEM)].
Tijdschrift voor diergeneeskunde    May 23, 1998   Volume 123, Issue 2 51 
Hesselink JW.No abstract available
Profiles of fragments after pulsed-field gel electrophoresis of cleaved genomic DNA from strains of Taylorella equigenitalis isolated from horses in Norway.
Microbiological research    July 1, 1997   Volume 152, Issue 2 217-220 doi: 10.1016/S0944-5013(97)80015-8
Matsuda M, Miyazawa T, Ishida Y, Moore JE.The genomic DNA of eight strains of Taylorella equigenitalis, isolated from seven Norwegian Trotters and a Norwegian pony with contagious equine metritis in Norway, was examined by pulsed-field gel electrophoresis after separate digestions with two restriction enzymes, namely, ApaI and NotI. The respective electrophoretic profiles of the fragments were essentially identical but differed from those of T. equigenitalis NCTC11184T and Kentucky 188. They also exhibited slight differences from profiles obtained from Japanese isolates. These results may possibly suggest a common genotype and a commo...
Epidemiologic aspects of Taylorella equigenitalis.
Theriogenology    April 15, 1997   Volume 47, Issue 6 1169-1177 doi: 10.1016/s0093-691x(97)00097-6
Parlevliet JM, Bleumink-Pluym NM, Houwers DJ, Remmen JL, Sluijter FJ, Colenbrander B.Contagious equine metritis (CEM) is a sexually transmissible disease in mares. Although the disease is commonly diagnosed by culturing the causative bacterium Taylorella equigenitalis (T. equigenitalis) . false negative results do occur. A recently developed Polymerase Chain Reaction (PCR) assay, however, appeared to be much more sensitive, with initial results indicating an unexpected high incidence of the agent in selected horses. In this study, samples from 107 randomly selected mares with no clinical signs of CEM submitted for conventional culture were all negative for T. equigenitalis . b...
Swabbing protocols in screening for contagious equine metritis.
The Veterinary record    March 15, 1997   Volume 140, Issue 11 268-271 
Watson ED.Outbreaks of contagious equine metritis in Britain during 1996 emphasised the importance of preventing the disease through full and widespread implementation of the Horserace Betting Levy Board's code of practice. The provision of satisfactory samples for testing represents an integral part of applying the code. Here, in an article commissioned by the British Equine Veterinary Association, Dr Elaine Watson describes the techniques involved.
Contagious equine metritis.
Comparative immunology, microbiology and infectious diseases    June 1, 1996   Volume 19, Issue 3 199-204 doi: 10.1016/0147-9571(96)00005-7
Timoney PJ.Contagious equine metritis (CEM) is a highly contagious venereal infection of equids caused by Taylorella equigenitalis, a bacterium with fastidious growth requirements. A disease of major international concern, CEM can be the cause of short-term infertility and, very rarely, abortion in mares. Unlike the mare, stallions exposed to T. equigenitalis do not develop clinical signs of disease. CEM is transmitted by direct or indirect venereal contact. The carrier state occurs in the mare and the stallion and carrier animals are frequently the source of infection for new outbreaks of the disease. T...
Differences between Taylorella equigenitalis strains in their invasion of and replication in cultured cells.
Clinical and diagnostic laboratory immunology    January 1, 1996   Volume 3, Issue 1 47-50 doi: 10.1128/cdli.3.1.47-50.1996
Bleumink-Pluym NM, ter Laak EA, Houwers DJ, van der Zeijst BA.The ability of Taylorella equigenitalis, the causative agent of contagious equine metritis, to invade and replicate in equine derm cells was studied. The kinetics of invasion and replication were determined for four T. equigenitalis strains. On the basis of these experiments, a simpler assay in which the invasive as well as the replicative properties of a particular strain could be determined was developed. This assay was used to characterize 32 strains, which had previously been typed by field inversion gel electrophoresis of genomic restriction fragments. The invasiveness of T. equigenitalis...
[Identification and diagnosis of Taylorella equigenitalis by a DNA amplification method (PCR)].
Schweizer Archiv fur Tierheilkunde    January 1, 1996   Volume 138, Issue 3 115-120 
Miserez R, Frey J, Krawinkler M, Nicolet J.A polymerase chain reaction (PCR) for identification of Taylorella equigenitalis was developed. The oligonucleotide primers are based on the DNA sequence of the rrs gene of T. equigenitalis, encoding for the 16S ribosomal RNA. Analysis of 21 strains of T. equigenitalis from England, USA and Switzerland showed an amplification product of 410 bp with identical Sau3A restriction profile. The sensitivity of the PCR-Assay was estimated to detect 50 to 500 bacteria of T. equigenitalis in a mixture with frequently found contaminants. Further analysis of culture from 60 genital swabs, taken in the cou...
Genetic homogeneity of Taylorella equigenitalis from Norwegian trotting horses revealed by chromosomal DNA fingerprinting.
Journal of clinical microbiology    January 1, 1995   Volume 33, Issue 1 233-234 doi: 10.1128/jcm.33.1.233-234.1995
Thoresen SI, Jenkins A, Ask E.Chromosomal DNA fingerprinting indicated that Norwegian Taylorella equigenitalis strains are genetically homogeneous and similar to some Swedish isolates but different from other European strains. As contagious equine metritis is rarely a serious disease in Norwegian horses, we conclude that the dominant T. equigenitalis strain in Norway is a genetically homogeneous clone of low virulence.
Genotyping of isolates of Taylorella equigenitalis from thoroughbred brood mares in Japan.
Veterinary research communications    January 1, 1995   Volume 19, Issue 4 265-271 doi: 10.1007/BF01839309
Miyazawa T, Matsuda M, Isayama Y, Samata T, Ishida Y, Ogawa S, Takei K, Honda M, Kamada M.Profiles of the genomic DNA of 104 strains of T. equigenitalis isolated from brood mares with contagious equine metritis in Hokkaido during the breeding seasons from 1980 to 1993, as well as those of five strains (SS28, EQ56, EQ59, EQ70 and HH139) previously isolated in Japan were examined after restriction digestion and crossed-field gel electrophoresis. These profiles were essentially identical to each other and the various isolates and strains appeared to have a common genotype, designated 'genotype J', with respect to two restriction enzymes, ApaI and NotI. These results suggest a common s...
Development and evaluation of PCR test for detection of Taylorella equigenitalis.
Journal of clinical microbiology    April 1, 1994   Volume 32, Issue 4 893-896 doi: 10.1128/jcm.32.4.893-896.1994
Bleumink-Pluym NM, Werdler ME, Houwers DJ, Parlevliet JM, Colenbrander B, van der Zeijst BA.A PCR for the detection of Taylorella equigenitalis, the causative agent of contagious equine metritis, was developed and evaluated. A genus-specific primer-probe set was derived from the 16S ribosomal DNA sequences. The PCR was specific and amplified a 585-bp product from all 64 available T. equigenitalis isolates. This PCR product hybridized with a specific probe in a dot spot assay. A variety of microorganisms from the genital tracts of horses or with a close phylogenetic relationship to T. equigenitalis did not yield a visible PCR product and were all negative in the dot spot hybridization...
Estimation of the size of the genome of Taylorella equigenitalis by crossed-field gel electrophoresis.
Veterinary research communications    January 1, 1994   Volume 18, Issue 2 99-102 doi: 10.1007/BF01839226
Matsuda M, Asami Y, Miyazawa T, Sugawara T, Kumano M, Isayama Y, Honda M.No abstract available
PCR-based detection of CEM agent.
The Veterinary record    October 9, 1993   Volume 133, Issue 15 375-376 doi: 10.1136/vr.133.15.375
Bleumink-Pluym NM, Houwers DJ, Parlevliet JM, Colenbrander B.No abstract available